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Chronic Inflammatory DiseaseSCORIC-ANCT05613712

Chronic Inflammatory Rheumatism: Management of Comorbidities in Ambulatory Medicine

An observational study of Chronic Inflammatory Disease, run by University Hospital, Grenoble at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Identification of factors limiting compliance with the recommendations established during the evaluation of the SCORIC population by the rheumatology department of the CHU Grenoble Alpes Read more about this study

Who is it for?
Ages 18 to 90 years
Conditions the study is for
Chronic Inflammatory Disease
What is being tested?
Patients and Referring physician
How many people
229 participants
Where
1 siteFrance
Study dates
11 Feb 2023to 4 May 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 90 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The SCORIC population targeted by the patient questionnaire represents all patients followed by the rheumatology department of the CHU Grenoble Alpes, having benefited from a holistic analysis of their disease and their comorbidities. The referring physician population will be generated from the medical records of the patients of the SCORIC cohort.

Who may be able to join

  • Patient cohort :
  • men and women over 18 years of age
  • Informed volunteers who have consented to participate in the study
  • have rheumatoid arthritis, spondyloarthritis or psoriatic arthritis
  • have been hospitalised in a day hospital in the rheumatology department of the Grenoble-Alpes University = SCORIC cohort of the department
  • Cohort of referring physicians :
  • volunteers who received informed information and consented to participate in the study
  • be the referring physician of a patient of the SCORIC cohort of the rheumatology department of the South Hospital of the CHU Grenoble-Alpes

Who cannot join

  • Patient cohort :
  • psychiatric pathologies or history of behavioural disorders
  • persons referred to in articles L1121-5 to L1121-8 of the Public Health Code
  • persons under guardianship or curatorship
  • not affiliated to the social security system
  • minors
Show all 10Show fewer
  • Refusal to participate by the patient and/or unreturned questionnaire
  • Cohort of referring physicians:
  • the physician is no longer the patient's referring physician
  • refusal of the doctor to participate and/or questionnaire not returned

Trial locations and contacts

1 site in 1 country.

France1 site
  • CHU Grenoble Alpes

    Grenoble, 38043

Other trials in France

About this study

Identification of factors limiting compliance with the recommendations established during the evaluation of the SCORIC population by the rheumatology department of the CHU Grenoble Alpes

Read the detailed description

In the rheumatology department of the CHU Grenoble Alpes, Professor Baillet and other rheumatologists have set up a holistic assessment of inflammatory rheumatism (rheumatoid arthritis, spondyloarthritis and psoriatic arthritis) and associated co-morbidities in a day hospital. Based on this assessment, a hospital report is drawn up summarising the patient's treatment options, which is then sent to the patient's referring physician. They analysed the first 100 patients in the cohort and showed that 98% of patients were not up to date with their care. Their longitudinal analysis shows that patients update two thirds of the recommendations made within 12 to 18 months. Therefore, the investigators would like to assess the applicability of this screening in these patients, through a questionnaire sent to the 400 patients of the cohort and to their treating physicians.

Being tested
Patients, Referring physician
Keywords
rheumatoid arthritis, spondyloarthropathy, spondylarthritis, ankylosing spondylitis, psoriatic arthritis, chronic inflammatory rheumatic diseases, comorbidities, continuity of patient care, patient compliance, adherence, non-adherence
Medical subject headings
Arthritis, Rheumatoid, Spondylarthropathies, Spondylarthritis, Spondylitis, Ankylosing, Arthritis, Psoriatic, Patient Compliance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PatientsOther

    Description by the patients through the questionnaire of the elements limiting the good ambulatory follow-up

  • Referring physicianOther

    Description by the referring physicians through the questionnaire of the elements limiting the applicability of the recommendations issued by the rheumatology department of the CHU Grenoble Alpes

Study groups in NCT05613712
Study groupRoleWhat they receive
PatientsPatients followed by the rheumatology department of the CHU Grenoble Alpes, constituting the SCORIC group
Receives: Other: Patients
Referring physicianPhysicians identified as the referring physician for patients in the SCORIC group
Receives: Other: Referring physician

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Identification of the factors limiting compliance with the recommendations established during the evaluation of the SCORIC population by the rheumatology department of the CHU Grenoble Alpes, through questionnaires

    Identification of the factors limiting compliance with the recommendations established during the evaluation of the SCORIC population by the rheumatology department of the CHU Grenoble Alpes

    Measured: 1 day

Secondary outcomes (2)
  1. Elements limiting the good ambulatory follow-up, according to the patients

    Description by the patients through the questionnaire of the elements limiting the good ambulatory follow-up

    Measured: 1 day

  2. Elements limiting the applicability of the recommendations issued by the rheumatology department of the CHU Grenoble Alpes, according to the patients

    Description by the referring physicians through the questionnaire of the elements limiting the applicability of the recommendations issued by the rheumatology department of the CHU Grenoble Alpes

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Nov 2022
  2. Study start11 Feb 2023
  3. Primary completion4 May 2023
  4. Study completion4 May 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
229 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05613712
Sponsor's protocol ID
38RC22.0355
Acronym
SCORIC-A
Status last verified
Dec 2025
First submitted
4 Nov 2022
Last updated
29 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Lagadou A, Gastaldi R, Vacher L, Baillet A. Gender influences adhesion to recommendations for optimal comorbidity screening and management of patients with chronic inflammatory rheumatic diseases starting a biological disease-modifying antirheumatic drug. RMD Open. 2024 Nov 11;10(4):e004364. doi: 10.1136/rmdopen-2024-004364. No abstract available.

    PubMed 39532462

Questions about this trial

What is this clinical trial studying?

An observational study of Chronic Inflammatory Disease, run by University Hospital, Grenoble at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Identification of the factors limiting compliance with the recommendations established during the evaluation of the SCORIC population by the rheumatology department of the CHU Grenoble Alpes, through questionnaires (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05613712, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Dec 2025.

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